Variant report

Variant	nsv880884
Chromosome Location	chr4:175439056-175453830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:857)
Chromatin interactive
region (count:9)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:175445435-175445665	K562	blood:	n/a	n/a
2	ATF1	chr4:175444081-175444464	K562	blood:	n/a	n/a
3	ATF3	chr4:175444189-175444447	K562	blood:	n/a	n/a
4	BACH1	chr4:175443570-175443858	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr4:175443428-175443853	GM12878	blood:	n/a	chr4:175443677-175443693
6	BHLHE40	chr4:175442908-175444261	K562	blood:	n/a	chr4:175443677-175443693
7	BHLHE40	chr4:175445482-175445725	K562	blood:	n/a	n/a
8	BHLHE40	chr4:175443462-175443846	HepG2	liver:	n/a	chr4:175443677-175443693
9	BHLHE40	chr4:175443469-175443773	A549	lung:	n/a	chr4:175443677-175443693
10	BRCA1	chr4:175443783-175444375	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr4:175445389-175445767	K562	blood:	n/a	n/a
12	CBX3	chr4:175443625-175444649	K562	blood:	n/a	n/a
13	CCNT2	chr4:175443310-175443912	K562	blood:	n/a	n/a
14	CEBPB	chr4:175440069-175440443	A549	lung:	n/a	chr4:175440290-175440303
15	CEBPB	chr4:175449375-175449740	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr4:175449435-175449712	K562	blood:	n/a	n/a
17	CEBPB	chr4:175449393-175449745	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:175449396-175449754	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:175449381-175449775	K562	blood:	n/a	n/a
20	CEBPB	chr4:175449377-175449773	K562	blood:	n/a	n/a
21	CEBPB	chr4:175449409-175449676	MCF-7	breast:	n/a	n/a
22	CEBPB	chr4:175449390-175449756	A549	lung:	n/a	n/a
23	CEBPB	chr4:175443317-175443491	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr4:175449396-175449751	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:175449416-175449742	IMR90	lung:	n/a	n/a
26	CHD2	chr4:175443638-175444009	HepG2	liver:	n/a	n/a
27	CHD2	chr4:175443516-175443966	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:175443570-175443770	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr4:175443654-175443813	GM12878	blood:	n/a	n/a
30	CHD2	chr4:175443624-175443960	K562	blood:	n/a	n/a
31	CREB1	chr4:175444049-175444553	K562	blood:	n/a	n/a
32	CREB1	chr4:175443611-175444633	K562	blood:	n/a	n/a
33	CREB1	chr4:175443329-175443895	A549	lung:	n/a	n/a
34	CTBP2	chr4:175442870-175443914	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:175443147-175443308	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:175443180-175443330	GM06990	blood:	n/a	n/a
37	CTCF	chr4:175443140-175443290	HEK293	kidney:	n/a	n/a
38	CTCF	chr4:175443480-175443656	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:175443160-175443310	Caco-2	colon:	n/a	n/a
40	CTCF	chr4:175443509-175443625	A549	lung:	n/a	n/a
41	CTCF	chr4:175443162-175443305	K562	blood:	n/a	n/a
42	CTCF	chr4:175443524-175443633	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:175443155-175443278	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:175443084-175443273	GM12878	blood:	n/a	n/a
45	CTCF	chr4:175443126-175443156	Lung_OC	lung:	n/a	n/a
46	CTCF	chr4:175443080-175443230	NHEK	skin:	n/a	n/a
47	CTCF	chr4:175443020-175443170	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr4:175443176-175443202	GM10266	blood:	n/a	n/a
49	CTCF	chr4:175443180-175443330	HRE	kidney:	n/a	n/a
50	CTCF	chr4:175443152-175443272	Gliobla	brain:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:175443752-175443802	MCF10A-Er-Src	breast:	n/a
2	chr4:175444096-175444146	Jurkat	blood:	n/a
3	chr4:175443407-175443457	AG09309	skin:	n/a
4	chr4:175443752-175443802	MCF10A-Er-Src	breast:	n/a
5	chr4:175444096-175444146	Jurkat	blood:	n/a
6	chr4:175443407-175443457	AG09309	skin:	n/a
7	chr4:175443867-175443917	ECC-1	luminal epithelium:	n/a
8	chr4:175444120-175444170	PFSK-1	brain:	n/a
9	chr4:175446087-175446137	HRPEpiC	eye:	n/a
10	chr4:175444948-175444998	Hepatocyte	liver:	n/a
11	chr4:175444482-175444532	AG09319	gingival:	n/a
12	chr4:175440325-175440375	HRCEpiC	kidney:	n/a
13	chr4:175446087-175446137	HRE	kidney:	n/a
14	chr4:175444268-175444318	CMK	blood:	n/a
15	chr4:175444482-175444532	CMK	blood:	n/a
16	chr4:175443752-175443802	NHBE	bronchial:	n/a
17	chr4:175444268-175444318	AG10803	skin:	n/a
18	chr4:175444181-175444231	HCPEpiC	choroid plexus:	n/a
19	chr4:175444948-175444998	U87	brain:	n/a
20	chr4:175444096-175444146	HepG2	liver:	n/a
21	chr4:175440325-175440375	AG09319	gingival:	n/a
22	chr4:175440325-175440375	NT2-D1	testis:	n/a
23	chr4:175444948-175444998	AoSMC	blood vessel:	n/a
24	chr4:175443569-175443619	HEK293	kidney:	embryo
25	chr4:175444120-175444170	NH-A	brain:	n/a
26	chr4:175444948-175444998	SKMC	muscle:	n/a
27	chr4:175444948-175444998	IMR90	lung:	fetal
28	chr4:175444948-175444998	SK-N-SH	brain:	n/a
29	chr4:175444096-175444146	SK-N-SH	brain:	n/a
30	chr4:175443243-175443293	U87	brain:	n/a
31	chr4:175444268-175444318	HCM	heart:	n/a
32	chr4:175443752-175443802	RPTEC	kidney:	n/a
33	chr4:175443243-175443293	LNCaP	prostate:	n/a
34	chr4:175444181-175444231	PrEC	prostate:	n/a
35	chr4:175444482-175444532	HNPCEpiC	eye:	n/a
36	chr4:175444482-175444532	GM12891	blood:	n/a
37	chr4:175444948-175444998	HCPEpiC	choroid plexus:	n/a
38	chr4:175440325-175440375	HEK293	kidney:	embryo
39	chr4:175444120-175444170	GM12891	blood:	n/a
40	chr4:175443867-175443917	HUVEC	blood vessel:	n/a
41	chr4:175444096-175444146	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:175446087-175446137	HRCEpiC	kidney:	n/a
43	chr4:175444120-175444170	NT2-D1	testis:	n/a
44	chr4:175443867-175443917	H1-hESC	embryonic stem cell:	embryo
45	chr4:175440325-175440375	Hepatocyte	liver:	n/a
46	chr4:175444181-175444231	IMR90	lung:	fetal
47	chr4:175443569-175443619	NHBE	bronchial:	n/a
48	chr4:175443243-175443293	NHBE	bronchial:	n/a
49	chr4:175443569-175443619	SK-N-MC	brain:	n/a
50	chr4:175444096-175444146	GM06990	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:99961025..99961526-chr4:175442445..175442945,2	MCF-7	breast:
2	chr4:175446994..175449489-chr4:175452030..175454343,2	K562	blood:
3	chr4:175446532..175448494-chr4:175449154..175453530,3	K562	blood:
4	chr4:175443375..175446407-chr4:175453659..175456708,4	K562	blood:
5	chr4:175446994..175449489-chr4:175452030..175454343,2	K562	blood:
6	chr4:175446532..175448494-chr4:175449154..175453530,3	K562	blood:
7	chr4:175441347..175443047-chr4:175456721..175458748,2	K562	blood:
8	chr4:175438441..175442290-chr4:175442561..175447463,6	K562	blood:
9	chr4:175442694..175445329-chr4:175449506..175451316,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP44-1	chr4:175447963-175448018	XLOC_003787
2	lnc-CEP44-1	chr4:175451245-175451355	XLOC_003787
3	lnc-CEP44-1	chr4:175447962-175448018	NONHSAT099320
4	lnc-CEP44-1	chr4:175444202-175444572	XLOC_003787
5	lnc-CEP44-1	chr4:175445332-175445678	XLOC_003787
6	lnc-CEP44-1	chr4:175447963-175448059	XLOC_003787
7	lnc-HPGD-1	chr4:175444852-175445773	ENSG00000250596.1
8	lnc-CEP44-1	chr4:175445216-175445813	NONHSAT099320

No data

Variant related genes	Relation type
ENSG00000251584	TF binding region
HPGD	TF binding region
ENSG00000251584	CpG island
HPGD	CpG island
ENSG00000164120	chromatin interactions
ENSG00000251584	chromatin interactions

Extended variants
information (count: 499 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17060589	chr4:175439056-175439057	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374801958	chr4:175439072-175439073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200777358	chr4:175439075-175439076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148441716	chr4:175439098-175439099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369541758	chr4:175439124-175439125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373121766	chr4:175439129-175439130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs138883930	chr4:175439147-175439148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs199975458	chr4:175439162-175439163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs376310920	chr4:175439163-175439164	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142173308	chr4:175439226-175439227	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144044660	chr4:175439270-175439271	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112048298	chr4:175439300-175439301	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557069841	chr4:175439309-175439310	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544182483	chr4:175439314-175439315	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577214924	chr4:175439350-175439351	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545880328	chr4:175439351-175439352	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs45444596	chr4:175439391-175439392	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs45525332	chr4:175439398-175439399	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs375377124	chr4:175439461-175439462	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369739252	chr4:175439469-175439470	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541990104	chr4:175439478-175439479	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139929832	chr4:175439487-175439488	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs45467793	chr4:175439583-175439584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143459773	chr4:175439666-175439667	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558217066	chr4:175439818-175439819	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575202502	chr4:175439961-175439962	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs17060592	chr4:175439996-175439997	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12500316	chr4:175440024-175440025	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191505899	chr4:175440025-175440026	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566546695	chr4:175440066-175440067	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182783997	chr4:175440071-175440072	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs45534931	chr4:175440095-175440096	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532568843	chr4:175440140-175440141	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs45600232	chr4:175440142-175440143	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537746782	chr4:175440143-175440144	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs562800003	chr4:175440152-175440153	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551606430	chr4:175440153-175440154	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187902101	chr4:175440190-175440191	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191379225	chr4:175440225-175440226	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs17060596	chr4:175440265-175440266	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs183550949	chr4:175440275-175440276	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572978995	chr4:175440328-175440329	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111659072	chr4:175440369-175440370	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199657484	chr4:175440382-175440383	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116141040	chr4:175440387-175440388	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555530808	chr4:175440396-175440397	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187799463	chr4:175440453-175440454	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544480166	chr4:175440513-175440514	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564769561	chr4:175440514-175440515	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs578206171	chr4:175440516-175440517	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175396000-175442800	Weak transcription	Esophagus	oesophagus
2	chr4:175410000-175440800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:175410800-175440000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr4:175420600-175441000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr4:175421000-175439200	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:175427400-175440600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr4:175427400-175443000	Weak transcription	Lung	lung
8	chr4:175427600-175441800	Weak transcription	Fetal Thymus	thymus
9	chr4:175428000-175439400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:175429400-175441200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr4:175429400-175442600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr4:175431000-175442400	Weak transcription	Fetal Intestine Large	intestine
13	chr4:175432800-175441600	Weak transcription	Placenta	Placenta
14	chr4:175433200-175442600	Weak transcription	Fetal Intestine Small	intestine
15	chr4:175435800-175442000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr4:175436400-175439200	Weak transcription	Primary T cells from cord blood	blood
17	chr4:175436800-175441400	Weak transcription	Stomach Mucosa	stomach
18	chr4:175437600-175439600	Enhancers	Liver	Liver
19	chr4:175438200-175439200	Weak transcription	A549	lung
20	chr4:175438200-175439400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr4:175438400-175440000	Enhancers	Primary hematopoietic stem cells	blood
22	chr4:175438400-175440200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:175438600-175439400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr4:175438600-175439600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr4:175438600-175439600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr4:175438600-175439800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:175438600-175440400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:175439200-175439600	Enhancers	Colon Smooth Muscle	Colon
29	chr4:175439200-175440000	Flanking Active TSS	A549	lung
30	chr4:175439200-175441000	Enhancers	Primary T cells from cord blood	blood
31	chr4:175439400-175439600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:175439400-175439600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:175439400-175439600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr4:175439400-175440200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr4:175439400-175440600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:175439400-175441600	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr4:175439600-175440000	Flanking Active TSS	Liver	Liver
38	chr4:175439600-175441400	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr4:175439600-175441800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr4:175439600-175442600	Weak transcription	Colon Smooth Muscle	Colon
41	chr4:175439600-175442800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:175439800-175441800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:175440000-175441200	Enhancers	A549	lung
44	chr4:175440000-175441400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr4:175440000-175444000	Active TSS	Liver	Liver
46	chr4:175440200-175441600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:175440200-175441800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr4:175440400-175441400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:175440600-175440800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr4:175440600-175440800	Flanking Active TSS	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links